1-{[(2S)-N-benzylpyrrolidin-2-yl]methyl}-4,5-diphenyl-1,3-dihydro-2H-imidazole-2-thione

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Chemical Name:1-{[(2S)-N-benzylpyrrolidin-2-yl]methyl}-4,5-diphenyl-1,3-dihydro-2H-imidazole-2-thione
CAS No.:1453114-85-6
Molecular Formula:C₂₇H₂₇N₃S
Molecular Weight:425.597
Hs Code.:

Synonyms:1-{[(2S)-N-benzylpyrrolidin-2-yl]methyl}-4,5-diphenyl-1,3-dihydro-2H-imidazole-2-thione

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Chemical Property of 1-{[(2S)-N-benzylpyrrolidin-2-yl]methyl}-4,5-diphenyl-1,3-dihydro-2H-imidazole-2-thione

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Technology Process of 1-{[(2S)-N-benzylpyrrolidin-2-yl]methyl}-4,5-diphenyl-1,3-dihydro-2H-imidazole-2-thione

There total 8 articles about 1-{[(2S)-N-benzylpyrrolidin-2-yl]methyl}-4,5-diphenyl-1,3-dihydro-2H-imidazole-2-thione which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 31.0%

: 1453114-74-3
1-{[(2S)-N-benzylpyrrolidin-2-yl]methyl}-4,5-diphenyl-1H-imidazole 3-oxide

: 1453114-85-6
1-{[(2S)-N-benzylpyrrolidin-2-yl]methyl}-4,5-diphenyl-1,3-dihydro-2H-imidazole-2-thione

Guidance literature:: With 2,2,4,4-tetramethylcyclobutane-1,3-dithione; In chloroform; at 0 - 20 ℃;
DOI:10.1016/j.tetasy.2013.07.013

Reference yield:

: 31795-93-4
N-benzyl-L-proline

: 1453114-85-6
1-{[(2S)-N-benzylpyrrolidin-2-yl]methyl}-4,5-diphenyl-1,3-dihydro-2H-imidazole-2-thione

Guidance literature:: Multi-step reaction with 6 steps

1.1: lithium aluminium tetrahydride / tetrahydrofuran / 0 - 20 °C

2.1: diethylazodicarboxylate; triphenylphosphine / tetrahydrofuran / 8.17 h / Reflux

3.1: hydrazine / ethanol / 2 h / Reflux

3.2: 0.5 h / Heating

4.1: methanol / 20 °C

5.1: acetic acid / ethanol / 24 h / 20 °C

6.1: 2,2,4,4-tetramethylcyclobutane-1,3-dithione / chloroform / 0 - 20 °C

With lithium aluminium tetrahydride; 2,2,4,4-tetramethylcyclobutane-1,3-dithione; acetic acid; triphenylphosphine; hydrazine; diethylazodicarboxylate; In tetrahydrofuran; methanol; ethanol; chloroform;
DOI:10.1016/j.tetasy.2013.07.013

Reference yield:

: 147-85-3,25191-13-3,37159-97-0,4305-67-3,4607-28-7
L-proline

: 1453114-85-6
1-{[(2S)-N-benzylpyrrolidin-2-yl]methyl}-4,5-diphenyl-1,3-dihydro-2H-imidazole-2-thione

Guidance literature:: Multi-step reaction with 7 steps

1.1: potassium hydroxide / isopropyl alcohol

2.1: lithium aluminium tetrahydride / tetrahydrofuran / 0 - 20 °C

3.1: diethylazodicarboxylate; triphenylphosphine / tetrahydrofuran / 8.17 h / Reflux

4.1: hydrazine / ethanol / 2 h / Reflux

4.2: 0.5 h / Heating

5.1: methanol / 20 °C

6.1: acetic acid / ethanol / 24 h / 20 °C

7.1: 2,2,4,4-tetramethylcyclobutane-1,3-dithione / chloroform / 0 - 20 °C

With lithium aluminium tetrahydride; 2,2,4,4-tetramethylcyclobutane-1,3-dithione; acetic acid; triphenylphosphine; potassium hydroxide; hydrazine; diethylazodicarboxylate; In tetrahydrofuran; methanol; ethanol; chloroform; isopropyl alcohol;
DOI:10.1016/j.tetasy.2013.07.013